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Serological Responses to Target Streptococcus pyogenes Vaccine Antigens in Patients With Proven Invasive β-Hemolytic
Kristyn Langworthy1, Michael Taggart1, Rosemary Smith2
1Department of Infectious Diseases, Fiona Stanley Fremantle Hospitals Group, Murdoch, Western Australia, Australia.
The Journal of Infectious Diseases
|October 9, 2024
Summary
Invasive β-hemolytic streptococcal infections are rising. This study found that patients with Strep A, C/G, or B infections developed significant antibody responses to key vaccine candidate antigens, suggesting potential for cross-species protection.
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Rising incidence of invasive β-hemolytic streptococcal (iBHS) infections necessitates preventative strategies.
- Vaccination against Streptococcus pyogenes (Strep A) could be enhanced by cross-species immunity against Streptococcus dysgalactiae subspecies equisimilis (SDSE) and Streptococcus agalactiae (GBS).
Purpose of the Study:
- To assess antibody responses to Strep A vaccine candidate antigens in patients with invasive infections.
- To investigate potential cross-species immune responses relevant for vaccine development.
Main Methods:
- Prospective observational study of adult patients with iBHS infections (Strep A, SDSE, GBS).
- Assay of antibody responses to 6 Strep A candidate antigens using acute and convalescent sera.
- Defined serological response as an increase of >0.2 log10 AU/mL.
Main Results:
- Strep A patients showed significant antibody responses to all 6 tested antigens.
- SDSE patients had significant responses to streptolysin-O, S. pyogenes adhesion and division protein, and C5a peptidase (ScpA).
- GBS patients showed significant responses to ScpA only.
Conclusions:
- Invasive Strep A infection elicits robust antibody responses to candidate vaccine antigens.
- Significant responses to C5a peptidase in SDSE and GBS patients suggest potential for cross-species protection.
- Further research is needed on cross-species protection and vaccine efficacy correlates.

